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Product Monograph Novel. Superior. Dual acting. Message from the Chairman’s Desk Dear Doctor, Greetings at a historic moment! We are indeed very pleased to announce the launch of our Novel, Superior, Dual Acting patented molecule LipaglynTM (Saroglitazar). This is the first drug ever to receive an approval for diabetic dyslipidemia - An Unmet Healthcare need. This is a landmark achievement not only for us, but for the entire healthcare fraternity in India. Discovered and developed by Zydus, Saroglitazar is a first-in-class molecule to be approved by the Drug Controller General of India to treat diabetic dyslipidemia or hypertriglyceridemia in type-2 diabetes not controlled by statins alone. Researched & developed over a span of 12 years, LipaglynTM is the first New Chemical Entity (NCE) from India to successfully complete the journey from the lab to the market. A team of over 400 dedicated research scientists at the Zydus Research Centre, Ahmedabad, guided the molecule through every stage, from the lab to the market. For patients with diabetic dyslipidemia, LipaglynTM is unique – • Superior safety profile - with a lower incidence of side events vs. current standard of care • Greater efficacy on lipid regulation (especially when taken in combination with statins) • Additionally, the drug also offers excellent glycemic control We are also embarking on a long term drug development program to globalize the molecule – in other emerging markets and in developed markets like Europe & USA. To familiarize you with our Novel, Superior & Dual Acting LipaglynTM, our medical team has compiled a product monograph specially for physicians like you. For further details you may visit www.lipaglyn.com Looking forward for your feedback on the therapeutic use of LipaglynTM. Warm Regards, Pankaj R. Patel Chairman and Managing Director Message from the Sr. VP’s Desk Dear Doctor, Greetings from Zydus Discovery!!! It is indeed a great pleasure to share this breakthrough of Zydus - LipaglynTM (Saroglitazar), India’s 1st NCE. This novel drug, discovered and developed through indigenous efforts, is approved for treating Diabetic Dyslipidemia – a global unmet healthcare need. This is a step forward in our commitment to serve the nation by strengthening the medical fraternity. The success of LipaglynTM can be a source of pride, not just for Zydus, but also for the Indian pharmaceutical industry and for the nation; encouraging more focus and investment on indigenous research. As you would know that today India is inching towards having the largest pool of diabetic patients globally. Moreover, nearly 80% of diabetic population have concomitant dyslipidemia and need a drug intervention for treatment. Our medical & R&D teams have compiled this product monograph with comprehensive information on Diabetic Dyslipidemia, current therapies and role of LipaglynTM in treatment of this condition. This monograph is comprised of three major sections– • Diabetic Dyslipidemia therapy area • LipaglynTM preclinical studies • LipaglynTM clinical studies Looking forward for your co-operation and guidance to enable LipaglynTM help every Diabetic Dyslipidemia patient in India lead a healthier life. Regards, M S Nath Sr. Vice President & Head SBU 2 (CVD) Preface Every fourth diabetic in the world is an Indian. As per an Indian Council of Medical Research (ICMR) study in 2011, the prevalence of diabetes has increased to 12-18% in urban India, 3-6% in rural India and another 14% having pre-diabetes. Translated into numbers, there were already 62.4 million diabetics and 77.2 million pre-diabetics in 2011 in India. The numbers are increasing exponentially. The reason is that the genetic susceptibility to develop diabetes is high in Indians. Indians have a low threshold for the risk factors like obesity, sedentary life habits and stress. These risk factors are applicable to all Indians irrespective of the place they live. Indians living in other countries too have a higher prevalence of diabetes compared to the natives and the Caucasian population. Diabetics have an increased cardiovascular risk. This risk gets exaggerated by lipid abnormalities additionally. Diabetics have an increased propensity to develop dyslipidemia (also known as ‘Atherogenic Diabetic Dyslipidemia’-ADD) characterized by high TG and/or low HDL-C and/ or small dense LDL-C. Indian type 2 diabetics are highly prone to be dyslipidemic, as a study found that 85.5% male, and, as high as 97.2% female Indian diabetics have dyslipidemia. Traditionally, diabetes and its accompanying dyslipidemia are managed by a variety of permutations and combinations of anti-diabetic and lipid-lowering drugs. The glycemic and lipid goals are not being met in the majority of patients because meeting these goals are a challenge. In the management of diabetes, insulin or the secretagogues cause hypoglycaemia, and the secretagogues can lead to exhaustion of the pancreatic beta cells. Metformin alone is not always sufficient, and the other insulin sensitizers like pioglitazone, acting by stimulating the nuclear peroxisome proliferator-activated receptors-γ (PPAR-γ) receptors, are under a cloud for their side effect profile. As far as lipids are concerned, statins at best are able to benefit 20-30% patients only. Fibrates, by stimulating the PPAR-α receptors, either alone or in combination with the statins, pose hazards of muscle toxicity. Niacin and fish-oils also do not meet the expectations. In such a scenario research got directed at developing dual PPAR-α/γ agonists which could address both the abnormalities of lipids and hyperglycemia in diabetic dyslipidemia. The potential of PPAR agonists to positively influence the cardiovascular disease risk in type 2 diabetics has remained an area of continuous medical interest. PPAR-α agonists (fenofibrate) and PPAR-γ agonist (pioglitazone) are approved respectively for lipid control and glycemic control in type 2 diabetes. However, increasing safety concerns with thiazolidinediones with regard to fluid retention, weight gain and congestive cardiac failure have resulted in new label warning for these agents. Hence, there was a strong need for a dual PPAR-α/γ agonist with beneficial effects in controlling both lipids and glycemic levels with all the necessary safety parameters. We bring to you the world’s first approved dual PPAR-α/γ agonist, LipaglynTM (saroglitazar), for your patients suffering from diabetic dyslipidemia, which has shown efficacy in improving both, the lipid as well as the glycemic parameters, with an excellent safety profile. Read the entire story of LipaglynTM in this monograph. Happy reading! Dr Anil J. Jaiswal VP – Medical Services Index Sr. No. Topic Page No. 1 Introduction: Burden of cardiovascular disease in India and its risk factors 11 2. Global and Indian diabetes prevalence 12 3. Diabetic dyslipidemia and its prevalence in India 13 4. Prevalence of hypertriglyceridemia in Indian diabetics 14 5. Classification of lipid parameters 15 6. Role of statins and fibrates in Atherogenic Diabetic Dyslipidemia 16 6.1 Statins 16 6.2 Fibric acid derivatives 16 7. Beyond LDL: The non-HDL-C guidelines 18 8. Triglycerides and CVD risk: Pathophysiology 20 9. Diabetic dyslipidemia, unmet needs and emerging role for dual PPAR-α/γ agonists 22 9.1 NCEP ATP III Guidelines 22 9.2 Emerging therapy approaches 24 10. Development of glitazars 26 10.1 What are PPARs? 26 10.2 Mechanism of action of PPAR agonists 26 10.3 Rationale for developing dual PPAR-α/γ agonists 26 10.4 History of development of dual PPAR-α/γ agonists 27 11. Introduction to LipaglynTM (Saroglitazar) 28 11.1 LipaglynTM – Physical and chemical properties 28 11.2 LipaglynTM - Formulation 29 12. LipaglynTM (Saroglitazar) - Pre-clinical studies 30 12.1 Preclinical safety and toxicity evaluation 32 12.2 Safety pharmacology 32 12.3 Effects on the cardiovascular system 33 12.4 Effects on the respiratory system 33 12.5 Supplemental and follow-up safety pharmacology studies 33 13. Clinical evidences of LipaglynTM (Saroglitazar) 35 13.1 Phase I studies 35 13.2 Phase II studies 36 13.3 Phase III studies 37 14. LipaglynTM (Saroglitazar) in the management of Atherogenic Diabetic Dyslipidemia 48 15. Prescribing information of LipaglynTM (Saroglitazar) 51 16. References 58 17. Abbreviations 61 1. Introduction: Burden of cardiovascular disease in India and its risk factors India accounts for 21% of the world’s global burden of disease. Non-communicable diseases (NCDs) are responsible for two-thirds of the total morbidity burden and about 53% of total deaths in India. This figure is expected to rise from 40.4% in 1990 to 59% by 2015. And, most importantly, two out of four leading NCDs in India are: Cardiovascular diseases (CVDs) Diabetes Mellitus (DM)1 India experienced the highest loss in potentially productive years of life worldwide. The leading cause of death was CVD; mostly affecting people aged 35-64 years. It has been calculated that, in 2000, 9.2 million years of productive life were lost in India.2 There are six leading risk factors associated with NCDs. They are: High blood glucose levels Altered lipid levels Physical inactivity Overweight/Obesity High blood pressure Tobacco use The prevalence of coronary heart disease (CHD) during 2003 in India was estimated to be 3-4% in rural areas (two-fold higher compared to 40 years ago), and 8-10% in urban areas (six-fold higher compared to 40 years ago), with a total affected population of 29.8 million (14.1 million in urban areas, and 15.7 million in rural areas). This estimate is comparable to the figure of 31.8 million affected, derived from extrapolations of the “Global Burden of Diseases Study”. These numbers likely underestimate the affected population as they do not account for those with silent myocardial infarction (MI) or otherwise asymptomatic CHD. In 1990, there were an estimated 1.17 million deaths from CHD in India, and the number was expected to almost double to 2.03 million by 2010.
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  • The Effect of Rosiglitazone on Overweight Subjects with Type 1 Diabetes

    The Effect of Rosiglitazone on Overweight Subjects with Type 1 Diabetes

    Clinical Care/Education/Nutrition ORIGINAL ARTICLE The Effect of Rosiglitazone on Overweight Subjects With Type 1 Diabetes SUZANNE M. STROWIG, MSN, RN the potentially serious consequences of PHILIP RASKIN, MD excessive weight gain and insulin- induced hypoglycemia, investigators con- tinue to search for treatments that address both the treatment of insulin deficiency as well as other metabolic abnormalities that OBJECTIVE — To evaluate the safety and effectiveness of rosiglitazone in the treatment of are associated with diabetes (5). overweight subjects with type 1 diabetes. Insulin resistance, a metabolic abnor- mality common in type 2 diabetes, ap- RESEARCH DESIGN AND METHODS — A total of 50 adult type 1 diabetic subjects 2 pears to be present in individuals with with a baseline BMI Ն27 kg/m were randomly assigned in a double-blind fashion to take insulin and placebo (n ϭ 25) or insulin and rosiglitazone 4 mg twice daily (n ϭ 25) for a period of 8 type 1 diabetes, as well. Although insulin months. Insulin regimen and dosage were modified in all subjects to achieve near-normal resistance in type 2 diabetes is generally glycemic control. associated with obesity, hypertension, dyslipidemia, and other metabolic disor- RESULTS — Both groups experienced a significant reduction in HbA1c (A1C) level (rosigli- ders, studies have shown that overweight tazone: 7.9 Ϯ 1.3 to 6.9 Ϯ 0.7%, P Ͻ 0.0001; placebo: 7.7 Ϯ 0.8 to 7.0 Ϯ 0.9%, P ϭ 0.002) and as well as normal-weight adults with type a significant increase in weight (rosiglitazone: 97.2 Ϯ 11.8 to 100.6 Ϯ 16.0 kg, P ϭ 0.008; 1 diabetes can have peripheral and he- Ϯ Ϯ ϭ ϭ placebo: 96.4 12.2 to 99.1 15.0, P 0.016).